FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OLDELFT SIMULIX-MC

K Number: K912466 · Decision Jun 28, 1991
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
69
Applicant Total
9
Review Days
24

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Basic Information

Device Name
OLDELFT SIMULIX-MC
K Number
K912466
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5840
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Oldelft Corp. of America
Date Received
June 4, 1991
Decision Date
June 28, 1991
Product Code
KPQ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPQ System, Simulation, Radiation Therapy

Similar 510(k) Clearances

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Other Clearances by Oldelft Corp. of America

K Number Device Name
K980296 OLDELFT DIGIDELCA
K973219 AMBER DU
K946128 SIMULIX-HP
K950037 N 800 HF
K932848 SIMULIX-MC CT EXTENSION
K923584 THERAPAX DXT 300 SERIES 3
K914784 PAPILLION PROCTOSCOPE
K892659 ELECTRODELCA